IP Library Granted Patent US 8,236,754
Granted Patent B2
US 8,236,754 · App. 12/478,593 · Granted Aug 7, 2012

Methods for improving the structure and function of arterioles

Assignee: The Regents of the University of California
View Patent ↗
Loading inventors, assignments & file history…
Monitor This Case
Get email alerts when status or documents change.
Order Certified Copies
Most orders are placed with the USPTO same day — all within 24 business hours.
Order via The Patent Place →
Pre-filled with this patent's details
Quick Facts
Patent No.
US 8,236,754
App. No.
12/478,593
Granted
Aug 7, 2012
Kind
B2
Abstract

The present invention relates to the unexpected finding that vessels smaller than even the smallest arteries (i.e. arterioles) thicken, become dysfunctional and cause end organ damage to tissues as diverse as the brain and the kidney. Methods are provided to improve the structure and function of arterioles and to preserve the function of end organs such as the brain and kidney. In various embodiments the methods involve administering to a mammal in need thereof “D” or “L” class A amphipathic helical peptides.

Claims (29)

1. A method of improving arteriole structure and/or function, said method comprising:

administering to a mammal in need thereof a peptide comprising the amino acid sequence D-W-L-K-A-F-Y-D-K-F-F-E-K-F-K-E-F-F (SEQ ID NO:7) in an amount sufficient to improve arteriole structure or function, wherein said mammal is a human diagnosed as having one or more conditions selected from the group consisting of age-related memory loss or impaired learning, impaired kidney function, and impaired alveolar function.

2. The method of claim 1 , wherein said arteriole is an arteriole in a kidney.

3. The method of claim 1 , wherein said arteriole is an arteriole in a brain.

4. The method of claim 1 , wherein said mammal is a human diagnosed as having memory loss or impaired learning.

5. The method of claim 1 , wherein said mammal is a human diagnosed as having impaired kidney function.

6. The method of claim 1 , wherein said mammal is a human diagnosed as having impaired alveolar function.

7. The method of claim 1 , wherein said mammal is a human not diagnosed as having or being at risk for atherosclerosis.

8. The method of claim 1 , wherein said peptide is in a unit dosage formulation.

9. The method of claim 1 , wherein the peptide is formulated for administration by a route selected from the group consisting of oral administration, nasal administration, rectal administration, intraperitoneal injection, intravascular injection, subcutaneous injection, transcutaneous administration, and intramuscular injection.

10. The method of claim 1 , wherein said administration is by a route selected from the group consisting of oral administration, nasal administration, rectal administration, intraperitoneal injection, intravascular injection, subcutaneous injection, transcutaneous administration, and intramuscular injection.

11. The method of claim 1 , wherein said peptide comprises a first protecting group on the amino terminus and/or a second protecting group on the carboxyl terminus.

12. The method of claim 1 , wherein said peptide is provided in combination with a pharmaceutically acceptable excipient.

13. The method of claim 1 , wherein said peptide is provided in a unit dosage formulation.

14. The method of claim 11 , wherein said first protecting group and said second protecting group are independently selected from the group consisting of acetyl, fatty acids, propionyl, formyl, amide, and ester.

15. The method of claim 11 , wherein said first protecting group is an acetyl.

16. The method of claim 11 , wherein said second protecting group is an amide.

17. The method of claim 11 , wherein said peptide has the formula Ac-D-W-L-K-A-F-Y-D-K-F-F-E-K-F-K-E-F-F-NH 2 (SEQ ID NO:7).

18. The method of claim 17 , wherein said peptide consists of all “D” amino acids.

19. The method of claim 17 , wherein said peptide consists of all “L” amino acids.

20. The method of claim 1 , wherein the amino acid sequence of said peptide consists of the sequence D-W-L-K-A-F-Y-D-K-F-F-E-K-F-K-E-F-F (SEQ ID NO:7).

21. The method of claim 20 , wherein said peptide consists of all “D” amino acids.

22. The method of claim 20 , wherein said peptide consists of all “L” amino acids.

23. A method of improving arteriole structure and/or function, said method comprising:

administering to a mammal in need thereof a peptide comprising the amino acid sequence D-W-L-K-A-F-Y-D-K-F-F-E-K-F-K-E-F-F (SEQ ID NO:7), or the retro, inverso, or retro-inverso forms of said amino acid sequence-in an amount sufficient to improve arteriole structure or function, wherein said mammal is a human diagnosed as having age-related memory loss or impaired learning, and said areteriole is an arteriole in a brain.

24. The method of claim 23 , wherein the amino acid sequence of said peptide consists of the sequence D-W-L-K-A-F-Y-D-K-F-F-E-K-F-K-E-F-F (SEQ ID NO:7).

25. A method of improving arteriole structure and/or function, said method comprising:

administering to a mammal in need thereof a peptide comprising the amino acid sequence D-W-L-K-A-F-Y-D-K-F-F-E-K-F-K-E-F-F (SEQ ID NO:7) or the retro, inverso, or retro-inverso forms of said amino acid sequence in an amount sufficient to improve arteriole structure or function, wherein said mammal is a human diagnosed as having impaired alveolar function.

26. The method of claim 25 , wherein the amino acid sequence of said peptide consists of the sequence D-W-L-K-A-F-Y-D-K-F-F-E-K-F-K-E-F-F (SEQ ID NO:7).

Assignments (2)
CONFIRMATORY LICENSE Recorded Feb 13, 2013
From: UNIVERSITY OF CALIFORNIA LOS ANGELES
To: NATIONAL INSTITUTES OF HEALTH (NIH), U.S. DEPT. OF HEALTH AND HUMAN SERVICES (DHHS), U.S. GOVERNMENT
Reel/Frame 029803/0382 →
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Dec 21, 2011
From: FOGELMAN, ALAN M.
To: THE REGENTS OF THE UNIVERSITY OF CALIFORNIA
Reel/Frame 027429/0771 →
Continuity (3)
Division 11296582 · Dec 6, 2005
Provisional Application 60634318 · Dec 6, 2004
Related Publication 20090286741A1 · Nov 19, 2009